3 Chloro 2 Fluorobenzyl Bromide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-Chloro-2-fluorobenzyl bromide
Chemical Formula C7H5BrClF
Molecular Weight 223.47
Appearance Typically a colorless to light - yellow liquid
Boiling Point Approximately 220 - 230 °C at normal pressure
Density Data may vary, but around 1.7 - 1.8 g/cm³
Solubility Soluble in organic solvents like dichloromethane, chloroform, insoluble in water
Vapor Pressure Low at room temperature
Stability Stable under normal conditions, but reacts with strong bases and nucleophiles
Chemical Formula C7H5BrClF
Molecular Weight 223.47
Appearance Colorless to light yellow liquid
Boiling Point Around 220 - 230 °C
Density Data may vary, but around 1.7 - 1.8 g/cm³
Solubility Slightly soluble in water, soluble in organic solvents like ether, dichloromethane
Flash Point Caution, likely flammable, flash point data may be around 90 - 100 °C
Odor Pungent, characteristic halogenated aroma
Stability Stable under normal conditions, but may react with strong oxidizing agents
FAQ

3-Chloro-2-fluorobenzyl chemical properties of bromide

3-Chloro-2-fluorobenzyl bromide is one of organic compounds. Its chemical properties are unique and quite active.

Looking at the characteristics of its halogen atom, this molecule contains three halogen atoms: chlorine, fluorine and bromine. Halogen atoms have electron-withdrawing properties, which can affect the stability of benzyl carbon positive ions, causing their nucleophilic substitution reaction activity to be different from that of normal substances. Among them, bromine atoms are very active in nucleophilic substitution reactions. Because the carbon-bromine bond energy is relatively small, it is easy to break, and it is often used as a check point for the attack of nucleophilic reagents. Nucleophilic reagents can attack benzyl carbon with lone pairs of electrons, and bro

Furthermore, although fluorine atoms are highly electronegative, their atomic radius is small, and the bonds formed with carbon atoms are very short and strong, which has a great impact on the distribution of molecular electron clouds, and the activity of ortho-chlorine atoms is also implicated. In some reactions, chlorine atoms can also participate in the reaction, but the activity is slightly less than that of bromine atoms.

Its chemical properties make it very useful in the field of organic synthesis. It can be used as an intermediate to form carbon-carbon bonds, carbon-heteroatomic bonds, etc. through nucleophilic substitution reactions, and synthesize many complex organic compounds. It can also participate in metal-catalyzed reactions, such as palladium-catalyzed cross-coupling reactions, which rely on the coordination of halogen atoms and metal catalysts to achieve precise connection between molecules, providing an effective way for the creation of new organic materials and drug molecules.

What are the main uses of 3-Chloro-2-fluorobenzyl bromide?

3-Chloro-2-fluorobenzyl bromide, this substance has a wide range of uses and is often a key intermediate in the field of organic synthesis. Due to its unique structure, the halogen atom has different activities and can initiate a variety of chemical reactions.

First, in the nucleophilic substitution reaction, the bromine atom is active and easy to be replaced by various nucleophilic reagents. Such as alcohol nucleophilic reagents, meet with it, and through this reaction, corresponding ether compounds can be generated, which is of great significance in the synthesis of medicine and the preparation of fine chemical products. For example, some ether drugs with specific pharmacological activities involve this step in the synthesis path.

Second, it also plays an important role in the construction of carbon-carbon bond reactions. During the Grignard reaction, 3-chloro-2-fluorobenzyl bromide can interact with magnesium to form Grignard reagents, which are then added to carbonyl compounds to achieve carbon chain growth and structural modification, providing an effective way for the construction of complex organic molecules. It is widely used in the fields of total synthesis of natural products.

Furthermore, in the field of materials science, it can be introduced into the main chain or side chain of polymer materials through specific reactions to give the material special properties. Such as changing the solubility and thermal stability of the material, or giving it responsiveness to specific substances, expanding the application range of the material.

In addition, in pesticide chemistry, using this as the starting material, through a series of reactions, pesticides with high insecticidal and bactericidal activities can be prepared. By adjusting the molecular structure to optimize its biological activity and environmental compatibility, it can help agricultural pest control and crop protection.

In summary, 3-chloro-2-fluorobenzyl bromide plays an indispensable role in many fields such as organic synthesis, materials science, medicine and pesticides due to its unique chemical properties, promoting development and progress in various fields.

What are the synthetic methods of 3-Chloro-2-fluorobenzyl bromide?

There are various ways to synthesize 3-chloro-2-fluorobenzyl bromide. First, it can be started from 3-chloro-2-fluorotoluene. First, a specific halogenating agent, such as N-bromosuccinimide (NBS), in the presence of an initiator such as benzoyl peroxide (BPO), in a suitable solvent such as carbon tetrachloride, is irradiated or heated to cause the methyl group to undergo a free radical bromination reaction. In this process, NBS can provide bromine radicals, and the BPO is thermally decomposed to produce a free radical initiator reaction, so the target product 3-chloro-2-fluorobenzyl bromide can be obtained.

Second, we can start from 3-chloro-2-fluorobenzoic acid. First reduce it to 3-chloro-2-fluorobenzyl alcohol, and commonly used reducing agents such as lithium aluminum hydride (LiAlH) or sodium borohydride (NaBH) react in suitable solvents such as anhydrous tetrahydrofuran. Subsequently, hydrobromic acid or phosphorus tribromide are used to convert the alcohol hydroxyl group into a bromine atom, thereby generating 3-chloro-2-fluorobenzyl bromide. Taking hydrobromic acid as an example, under heating conditions, the alcohol undergoes a nucleophilic substitution reaction with hydrobromic acid, and the hydroxyl group is replaced by bromine.

Or derived from the corresponding phenolic compound. First, the phenolic hydroxyl group is properly protected, then chlorine and fluorine substituents are introduced, and then the benzyl structure is constructed through a series of reactions, and finally bromine atoms are introduced. This route requires fine design of the reaction steps and conditions to ensure the smooth progress of each step and good selectivity. During the synthesis process, attention should be paid to the precise control of the reaction conditions, such as temperature, reaction time, reagent dosage, etc., to improve the yield and purity of the product.

3-Chloro-2-fluorobenzyl bromide need to pay attention to when storing and transporting

3-Chloro-2-fluorobenzyl bromide is also an organic compound. When storing and transporting it, many matters must be paid attention to.

First storage, this compound is active and sensitive to environmental factors. First, it needs to be stored in a cool place. Because the temperature is too high, it is easy to cause chemical reactions, or cause undesirable changes such as decomposition and polymerization, which will damage its quality. The temperature should be controlled within a specific range, such as usually 2-8 ° C, so that its chemical stability can be maintained. Second, it must be placed in a dry place. Because it encounters water or moisture, or undergoes hydrolysis, other substances are formed and its chemical composition and properties are changed. Therefore, the humidity of the storage environment should be strictly controlled, and auxiliary means such as desiccants can be used to maintain the dry environment. Third, it should be stored in a well-ventilated place. This compound may be volatile to a certain extent. If the ventilation is not smooth, its volatile gas will gather in one place, which is not good for the health of the user. Second, it may cause safety hazards such as fire and explosion due to high concentration.

Second, during transportation, ensuring its stability and safety is of paramount importance. Packaging must be tight. Suitable packaging materials should be selected, which must be resistant to the corrosion of this compound and can effectively block the interference of external factors. Commonly used, such as glass containers, because of their stable chemical properties, it is not easy to react with compounds; however, glass is fragile and needs to be supplemented with cushioning materials to prevent collision and breakage during transportation. If plastic containers are used, specific materials should also be selected to ensure that no adverse phenomena such as swelling with compounds occur. Furthermore, during transportation, temperature and vibration should also be paid attention to. Large fluctuations in temperature should be avoided as much as possible, and at the same time, the vibration of the transportation vehicle should be slowed down. Due to excessive vibration, or changes in the molecular structure of the compound, its quality will be affected. And when transporting, it should be properly marked in accordance with relevant regulations, indicating its chemical properties and dangerous characteristics, so that transporters and regulators can clearly adopt corresponding protection and emergency measures. In summary, 3-chloro-2-fluorobenzyl bromide has strict requirements for temperature, humidity, ventilation, packaging, etc. during storage and transportation, so as to ensure its quality and safety.

3-Chloro-2-fluorobenzyl bromide affect the environment and human health

3-Chloro-2-fluorobenzyl bromide is also an organic compound. Its impact on the environment and human health needs to be investigated in detail.

First of all, its impact on the environment. If this substance is released in nature, in soil and water, or difficult to degrade, and gradually accumulate. In soil, or hinder the development of plant roots, causing nutrient uptake to be blocked, growth to be trapped, leaves to wither. In water, or toxic and aquatic organisms, such as fish, turtles, shrimp and crabs, damage their gills, lungs and other respiratory organs, causing breathing difficulties, and even death. And it may be transmitted through the food chain, from lower organisms to higher organisms, the concentration gradually rises, the harm is even worse, and eventually the ecological balance is disrupted, and the biodiversity is sharply reduced.

Re-discuss its harm to human health. If a person is infected by breathing, skin contact or accidental ingestion, the harm is immediate. Breathing in, or stabbing the respiratory tract, causing cough, asthma, chest tightness, and even damage the function of the lungs, causing respiratory diseases. Through skin contact, or cause skin allergies, itching, redness and swelling, long-term contact will break the skin and rot, poison into the bloodline. If ingested by mistake, it may injure the stomach, cause abdominal pain, diarrhea, vomiting, and poison into the blood, travel around the body, damage the liver, kidney, brain and other important organs, affect the body's metabolism, detoxification and nerve conduction function, and even endanger life.

Therefore, the production, use and disposal of 3-chloro-2-fluorobenzyl bromide should be done with caution to protect the environment and human well-being.